Otoraplin anticorps

N° du produit ABIN7230424

L’anticorps anti-Otoraplin Polyclonal Lapin est utilisé pour la détection de Otoraplin dans des échantillons de Humain et Souris. Il a été validé pour ELISA et WB.

Aperçu rapide pour Otoraplin anticorps (ABIN7230424)

Antigène: Otoraplin (OTOR)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Otoraplin est non-conjugé

Application: ELISA, Western Blotting (WB)

Détail du produit anti-Otoraplin anticorps

Fonction: OTOR Polyclonal Antibody

Specificité: The antibody detects endogenous levels of OTOR protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human OTOR protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Otoraplin

Antigène: Otoraplin (OTOR)

Autre désignation: OTOR

Sujet: Rabbit Anti-OTOR Polyclonal Antibody,Otoraplin, Fibrocyte-derived protein, Melanoma inhibitory activity-like protein,This gene encodes a member of the melanoma-inhibiting activity gene family. The encoded protein is secreted via the Golgi apparatus and may function in cartilage development and maintenance. A frequent polymorphism in the translation start codon of this gene can abolish translation and may be associated with forms of deafness.,OTOR

Poids moléculaire: observerd band 14kDa

ID gène: 56914

UniProt: Q9NRC9

Pathways: Sensory Perception of Sound, Regulation of Carbohydrate Metabolic Process